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Product Image-1B1634-0.1KU

VWR®, Cod Uracil-DNA glycosylase

Supplier: VWR Chemicals
Description: Uracil-DNA glycosylase (UNG), cod is a thermolabile recombinant enzyme produced in <i>E. coli</i> (ung-) using a modified ung gene derived from Atlantic cod. It degrades uracil-containing single- and double-stranded DNA, but not RNA or thymidine-containing DNA, by hydrolysing the N-glycosidic bond between deoxyribose sugar and the base in uracil. This generates alkaline-sensitive apyramidinic sites in the DNA that will be cleaved upon a combination of alkaline conditions and high temperature.

MSDS

Product Image-113-9205

Mob caps, non woven, PP

Catalog Number: (113-9205)
Supplier: HUBEI ORIENT INTL TRADING
Description: Disposable pleated mob caps made from soft non woven PP.
UOM: 1 * 1.000 items
Product Image-116-0473

Prohibition signs

Supplier: Brady
Description: Prohibition signs must have a black diagram encircled by a red band and dissected by a red diagonal bar.

Image Unavailable-BOSSBS-11362R-CY3

Anti-SNAP23 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-11362R-CY3)
Supplier: Bioss
Description: Essential component of the high affinity receptor for the general membrane fusion machinery and an important regulator of transport vesicle docking and fusion.
UOM: 1 * 100 µl
Product Image-BRDY237556

Thermal transfer ribbon for printer, R7942 series

Catalog Number: (BRDY237556)
Supplier: Brady
Description: Waxed ribbon for general use on paper and for temporary identification.
UOM: 1 * 1 items
Product Image-216-8227

Jars, wide mouth, with screw caps, Nalgene®

Supplier: Thermo Fisher Scientific
Description: PC, clear with white PP screw cap, PMP, clear with white PP screw cap or PPCO, translucent with white PP screw cap.

Environmentally Preferable

Product Image-444-1423

VWR® Microplate Shaker, 230 V

Catalog Number: (444-1423)
Supplier: VWR Collection
Description: <p>VWR® microplate shakers feature variable-speed, microprocessor control, providing reliable, uniform mixing action. Ideal for immunoassays and general microplate shaking and includes a platform to accommodate four plates.</p>
UOM: 1 * 1 items

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Image Unavailable-BOSSBS-9013R-FITC

Anti-EFHC1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (BOSSBS-9013R-FITC)
Supplier: Bioss
Description: Defects in EFHC1 are the cause of juvenile myoclonic epilepsy type 1 (EJM1) [MIM:254770]. EJM1 is a subtype of idiopathic generalized epilepsy (IGE). Patients have afebrile seizures only, with onset in adolescence (rather than in childhood) and myoclonic jerks which usually occur after awakening and are triggered by sleep deprivation and fatigue.Genetic variations in EFHC1 are the cause of susceptibility to juvenile absence epilepsy type 1 (JAE1) . JAE is a subtype of idiopathic generalized epilepsy characterized by onset occurring around puberty, absence seizures, generalized tonic-clonic seizures (GTCS), GTCS on awakening, and myoclonic seizures.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9013R-A647

Anti-EFHC1 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-9013R-A647)
Supplier: Bioss
Description: Defects in EFHC1 are the cause of juvenile myoclonic epilepsy type 1 (EJM1) [MIM:254770]. EJM1 is a subtype of idiopathic generalized epilepsy (IGE). Patients have afebrile seizures only, with onset in adolescence (rather than in childhood) and myoclonic jerks which usually occur after awakening and are triggered by sleep deprivation and fatigue.Genetic variations in EFHC1 are the cause of susceptibility to juvenile absence epilepsy type 1 (JAE1) . JAE is a subtype of idiopathic generalized epilepsy characterized by onset occurring around puberty, absence seizures, generalized tonic-clonic seizures (GTCS), GTCS on awakening, and myoclonic seizures.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9013R-A350

Anti-EFHC1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Catalog Number: (BOSSBS-9013R-A350)
Supplier: Bioss
Description: Defects in EFHC1 are the cause of juvenile myoclonic epilepsy type 1 (EJM1) [MIM:254770]. EJM1 is a subtype of idiopathic generalized epilepsy (IGE). Patients have afebrile seizures only, with onset in adolescence (rather than in childhood) and myoclonic jerks which usually occur after awakening and are triggered by sleep deprivation and fatigue.Genetic variations in EFHC1 are the cause of susceptibility to juvenile absence epilepsy type 1 (JAE1) . JAE is a subtype of idiopathic generalized epilepsy characterized by onset occurring around puberty, absence seizures, generalized tonic-clonic seizures (GTCS), GTCS on awakening, and myoclonic seizures.
UOM: 1 * 100 µl
Product Image-BOSSBS-5159R

Anti-Fast skeletal Myosin Rabbit Polyclonal Antibody

Catalog Number: (BOSSBS-5159R)
Supplier: Bioss
Description: Myosin is a highly conserved, ubiquitously expressed protein that interacts with Actin to generate the force for cellular movements. Conventional Myosins are hexameric proteins consisting of two heavy chain subunits, a pair of non-phosphorylatable light chain subunits and a pair of phosphorylatable light chain subunits. Three general classes of Myosin have been cloned: smooth muscle Myosins, striated muscle Myosins and non-muscle Myosins . Contractile activity in smooth muscle is regulated by the calcium/calmodulin-dependent phosphorylation of Myosin light chain (MLC) by Myosin light chain kinase. Myosin heavy chains, which are encoded by the MYH gene family, contain Actin-activated ATPase activity which generates the motor function of Myosin. Myosin heavy chains were initially isolated from a human fetal skeletal muscle and are the major determinant in the speed of contraction of skeletal muscle. Various isoforms of myosin heavy chains are differentially expressed depending on the functional activity of the muscle.
UOM: 1 * 100 µl
Image Unavailable-ENZOBMLEI1171000

RO 20-1724 ≥99% (by TLC)

Supplier: ENZO LIFE SCIENCES
Description: Selective, potent cAMP-specific phosphodiesterase inhibitor (PDE IV, IC50=2µM). Inhibits superoxide generation and platelet aggregation stimulated by arachidonic acid. Also inhibits fMLP-induced neutrophil adhesion to vascular endothelial cells.

Product Image-786-383

femtoCHROMO™- AP Substrate for chromogenic detection

Supplier: G-Biosciences
Description: A ready to use modified BCIP (5-Bromo-4-Chloro-3’-Indolyphosphate p-Toluidine salt) and NBT (Nitro-Blue Tetrazolium Chloride) substrate that generates a black-purple insoluble precipitate in the presence of alkaline phosphatase.

Product Image-BRDY142957

Labels for BBP33 printers, type B-486

Supplier: Brady
Description: Metallised polyester labels for product labelling, asset tracking and general industrial ID.

Image Unavailable-BOSSBS-9013R-CY5.5

Anti-EFHC1 Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (BOSSBS-9013R-CY5.5)
Supplier: Bioss
Description: Defects in EFHC1 are the cause of juvenile myoclonic epilepsy type 1 (EJM1) [MIM:254770]. EJM1 is a subtype of idiopathic generalized epilepsy (IGE). Patients have afebrile seizures only, with onset in adolescence (rather than in childhood) and myoclonic jerks which usually occur after awakening and are triggered by sleep deprivation and fatigue.Genetic variations in EFHC1 are the cause of susceptibility to juvenile absence epilepsy type 1 (JAE1) . JAE is a subtype of idiopathic generalized epilepsy characterized by onset occurring around puberty, absence seizures, generalized tonic-clonic seizures (GTCS), GTCS on awakening, and myoclonic seizures.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9013R-A555

Anti-EFHC1 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalog Number: (BOSSBS-9013R-A555)
Supplier: Bioss
Description: Defects in EFHC1 are the cause of juvenile myoclonic epilepsy type 1 (EJM1) [MIM:254770]. EJM1 is a subtype of idiopathic generalized epilepsy (IGE). Patients have afebrile seizures only, with onset in adolescence (rather than in childhood) and myoclonic jerks which usually occur after awakening and are triggered by sleep deprivation and fatigue.Genetic variations in EFHC1 are the cause of susceptibility to juvenile absence epilepsy type 1 (JAE1) . JAE is a subtype of idiopathic generalized epilepsy characterized by onset occurring around puberty, absence seizures, generalized tonic-clonic seizures (GTCS), GTCS on awakening, and myoclonic seizures.
UOM: 1 * 100 µl
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organisation. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
Product(s) marked with this symbol are discontinued - sold till end of stock. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service on +353 1 8822222.
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